Search the 30 jobs at Cellares

The Recruiting Coordinator will facilitate the recruitment process by scheduling interviews, managing candidate interactions, and assisting with onboarding. This role involves logistical support and collaboration with the recruiting team to enhance the candidate experience and streamline processes.

The Sales Enablement Manager will enhance the effectiveness of Business Development teams by providing necessary resources, training, and support. Responsibilities include overseeing CRM utilization, mapping sales processes, developing sales enablement programs, monitoring performance metrics, managing sales collateral, and facilitating training sessions.

The Platform Scientist will collaborate with engineering and biology teams to develop and optimize cell therapy manufacturing processes. Responsibilities include designing and executing experiments, analyzing results, authoring technical documents, performing laboratory activities, and developing training materials. The role requires strong communication and collaboration skills, particularly in a fast-paced environment.

The Research Associate will support the design and execution of experiments related to cell therapy process development, optimize hardware and software performance, and collaborate across teams to advance manufacturing capabilities. Key responsibilities include analyzing results, contributing to technical documents, and developing training materials for new team members.

The Scientist in Process Development will design and execute experiments to improve the cell therapy manufacturing platform. They will collaborate with various teams, author technical documents, analyze results, and support troubleshooting. The ideal candidate has a degree in bioengineering, chemical engineering, biology, or related field and experience in the cell and gene therapy field. Strong communication, technical skills, and a self-motivated mindset are required.

The Human Resources Manager will establish and implement HR best practices, maintain daily functions of the HR department, assist employees with benefits and payroll inquiries, draft company policies, ensure compliance with employment laws, and manage employee relations.

The Senior Systems Integration Engineer will lead integration testing, troubleshooting, and improve advanced cell therapy systems. Responsibilities include executing complex experiments, generating technical documentation, and collaborating with cross-functional teams to enhance performance and efficiency of technology platforms.

The Senior Applications Scientist will work on cell therapy manufacturing processes, design experiments, provide technical support, and collaborate across departments. They will also analyze data, train junior members, and author technical documents.

The Consumable Quality Engineer will lead the testing and validation of consumables, ensuring compliance with ISO 10993 and USP Class VI standards. Responsibilities include developing qualification plans, executing a range of tests, coordinating with external labs, analyzing test results, and collaborating across departments.

The Senior Manager of Operational Technology will oversee technical operations and infrastructure in an industrial and cell therapy lab, ensuring 24x7 operational support. Responsibilities include managing OT systems, developing implementation plans, ensuring compliance with security best practices, troubleshooting production issues, and delivering training for OT staff, while interacting with senior leadership and business functions to align priorities.

The Automation Engineer will support the deployment and optimization of automated QC testing workflows, validate methods for sample preparation and analysis, monitor system performance, conduct validation testing, and develop troubleshooting methodologies. They will work collaboratively with cross-functional teams and contribute to system documentation and training.

Seeking a Senior Analytical Transfer Specialist to lead analytical method transfers, evaluation, and support for cell therapy QC operations. Responsibilities include authoring procedures, contributing to regulatory submissions, and providing technical leadership. Requires a Bachelor's degree and 4+ years of experience in biologics/gene therapy with knowledge of QC principles and relevant analytical methods.

Seeking a Senior Process Engineer to contribute to the development of an advanced cell therapy manufacturing platform. Responsibilities include technology transfer, process development, compliance, scalability, and driving process automation solutions. Must have 5+ years of experience in biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy.

Seeking a VP, CMC Process Sciences to oversee establishment and execution of CMC development plans for cell and gene therapy products. Responsible for providing CMC leadership, collaborating with stakeholders, and driving effective communication and coordination across functional groups.

The VP of Finance will lead operational and financial planning cycles, oversee FP&A activities such as forecasting and budgeting, provide insights on project profitability, conduct internal cash flow analysis, and prepare financial presentations for stakeholders.

Seeking an experienced Senior Data Engineer to lead the design, development, and management of scalable data pipelines and architecture for a cell therapy manufacturing platform. Responsibilities include data pipeline implementation, collaboration with cross-functional teams, data preprocessing for machine learning models, and documentation of processes. Requirements include a Bachelor's or Master's degree in Computer Science, 6+ years of data engineering experience, proficiency in Azure services, programming skills in Python or C#, and experience in data visualization tools and data governance.

The Manager of Analytical Operations will oversee a team of scientists and analysts, manage assay execution and data analysis, ensure compliance with regulatory standards, and troubleshoot operational issues. Responsibilities include method transfer, team management, and aiding in regulatory submissions.

The CMC Program Manager at Cellares is responsible for managing project timelines and coordinating activities related to cell therapy manufacturing, acting as a liaison between multiple cross-functional teams. Responsibilities include budget management, risk mitigation, regulatory filings support, and ensuring customer satisfaction through effective communication and problem-solving.

The Senior Process Engineer will lead technology transfer activities for cGMP manufacturing, focusing on process automation, compliance, and scalability. Responsibilities include developing project plans, supporting late-stage process development, defining user requirements for equipment, conducting root cause analyses, and collaborating with stakeholders. This role requires expertise in technology transfer and manufacturing science.

The Director of Product Management will oversee the entire product lifecycle, from ideation to launch, collaborate with the R&D team, analyze market trends, and ensure alignment with company strategy. The role requires both high-level strategy and hands-on execution in a dynamic environment.